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Clinical trials for Tendinitis

The European Union Clinical Trials Register   allows you to search for protocol and results information on:
  • interventional clinical trials that were approved in the European Union (EU)/European Economic Area (EEA) under the Clinical Trials Directive 2001/20/EC
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    Clinical Trials Information System (CTIS).

    The EU Clinical Trials Register currently displays   43881   clinical trials with a EudraCT protocol, of which   7295   are clinical trials conducted with subjects less than 18 years old.   The register also displays information on   18700   older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).

    Phase 1 trials conducted solely on adults and that are not part of an agreed paediatric investigation plan (PIP) are not publicly available (see Frequently Asked Questions ).  
     
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    17 result(s) found for: Tendinitis. Displaying page 1 of 1.
    EudraCT Number: 2010-020513-87 Sponsor Protocol Number: Q03-09-01 Start Date*: 2010-09-02
    Sponsor Name:FIDIA
    Full Title: A randomized, placebo-controlled, double-blind study on the intensity and duration of efficacy of sodium hyaluronate therapy (500-730 KDa) (HYALGAN) in the conservative treatment of Achilles tendin...
    Medical condition: Achilles tendinopathy.
    Disease: Version SOC Term Classification Code Term Level
    9.1 10000433 LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: View results
    EudraCT Number: 2004-002856-32 Sponsor Protocol Number: 7148L05 Start Date*: 2004-11-18
    Sponsor Name:ZAMBON GROUP
    Full Title: Ketoprofen TDS patch Keofix in the treatment of flare-ups of non articular rheumatisms. A double blind, double dummy study vs oral ketoprofen retard 200 mg capsules
    Medical condition: non articular rheumatism
    Disease: Version SOC Term Classification Code Term Level
    6.1 10043255 PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: View results
    EudraCT Number: 2015-003587-36 Sponsor Protocol Number: 684/MODREC/15 Start Date*: 2016-04-13
    Sponsor Name:Directorate of Defence Rehabilitation
    Full Title: Chronic Tendinopathy: The Biomechanical Associations and EfFicacy of Injectable Therapy (BE FIT) Study
    Medical condition: Chronic degenerative Achilles and patella tendinopathy patients, with neovascularisation on USS, who have failed best practice rehabilitation including Eccentric Loading (EL), Heavy Slow Resistance...
    Disease: Version SOC Term Classification Code Term Level
    18.1 100000004859 10000433 Achilles tendinitis LLT
    18.1 100000004859 10034123 Patellar tendinitis LLT
    Population Age: Adults Gender: Male
    Trial protocol: GB (GB - no longer in EU/EEA)
    Trial results: (No results available)
    EudraCT Number: 2010-021869-73 Sponsor Protocol Number: 33178 Start Date*: 2011-01-25
    Sponsor Name:OrthoCell Pty Ltd
    Full Title: The value of Autologous Tenocyte Implantation in patients with chronic Achilles tendinopathy: a double-blind randomised clinical trial
    Medical condition: Chronic midportion Achilles tendinopathy
    Disease: Version SOC Term Classification Code Term Level
    12.1 10000433 Achilles tendinitis LLT
    12.1 10000435 Achilles tendon injury LLT
    12.1 10048602 Achilles tendon discomfort LLT
    12.1 10050471 Achilles tendon pain LLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: NL (Completed)
    Trial results: (No results available)
    EudraCT Number: 2015-005421-40 Sponsor Protocol Number: RCSI-1764 Start Date*: 2016-06-14
    Sponsor Name:Royal College of Surgeons in Ireland
    Full Title: The use of topical Glyceryl Trinitrate (GTN) and eccentric exercises in the treatment of mid portion Achilles Tendinopathy: a randomised placebo controlled trial
    Medical condition: Achilles tendinopathy
    Disease: Version SOC Term Classification Code Term Level
    18.1 100000004859 10050471 Achilles tendon pain LLT
    18.1 100000004859 10050129 Achilles tendon thickening LLT
    18.1 100000004863 10000435 Achilles tendon injury LLT
    18.1 100000004859 10000433 Achilles tendinitis LLT
    18.1 100000004859 10000441 Achilles tendonitis LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IE (Completed)
    Trial results: View results
    EudraCT Number: 2004-005087-24 Sponsor Protocol Number: Version 2 23/03/2005. Start Date*: 2005-07-11
    Sponsor Name:University Hospitals of Leicester NHS Trust
    Full Title: CIMETIDINE IN THE TREATMENT OF CALCIFIC SUPRASPINATUS TENDINITIS- A TRIAL OF CIMETIDINE 200mg B.D IN THE RESOLUTION OF CALCIFICATION IN THE SUPRASINATUS TENDON.
    Medical condition: CALCIFIC SUPRASPINATUS TENDINITIS
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: GB (Completed)
    Trial results: View results
    EudraCT Number: 2015-003238-29 Sponsor Protocol Number: BRN-C-2015-03 Start Date*: 2016-04-06
    Sponsor Name:Fundación Sociedad Española de Médicos de Atención Primaria (SEMERGEN)
    Full Title: Pilot phase II clinical trial, randomized, double-blind, controlled, single-center study to evaluate the efficacy and safety of Solanum malacoxylon 9CH in patients with calcific tendinitis of shoulder
    Medical condition: Calcific tendinitis of shoulder
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: ES (Completed)
    Trial results: View results
    EudraCT Number: 2009-011339-11 Sponsor Protocol Number: PRP-H1 Start Date*: 2009-07-07
    Sponsor Name:daniel pacha vicente
    Full Title: Estudio clínico prospectivo y randomizado comparando la inyección subacromial de plasma rico en plaquetas o de betametasona y bupivacaina en la tendinosis del manguito rotador del hombro.
    Medical condition: tendinitis cronica o tendinosis del manguito rotador del hombro
    Disease: Version SOC Term Classification Code Term Level
    9 10039228 Rotator cuff syndrome of shoulder and allied disorders LLT
    9 10057904 Rotator cuff tendinitis LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2016-001262-28 Sponsor Protocol Number: MSC-TENDO-2015 Start Date*: 2017-08-21
    Sponsor Name:Institut de Terapia Regenerativa Tissular S.L. (ITRT)
    Full Title: Treatment of Refractory Patellar Tendinopathy with MSV *. Comparative study with P-PRP *MSV are bone marrow autologous mesenchymal stem cells, selected and cultured under Good manufacturing Practic...
    Medical condition: Patients diagnosed with patellar tendinopathy with a minimum of 4 months evolution and have presented two acute episodes, refractory to standard treatments present a gap equal or greater than 3 mm ...
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004859 10034123 Patellar tendinitis LLT
    Population Age: Adults Gender: Male
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2007-001709-85 Sponsor Protocol Number: 10.05.7 Start Date*: 2007-11-13
    Sponsor Name:South Eastern Health and Social Care Trust
    Full Title: Treatment of Shoulder Capsulitis by single or Multiple Corticosteroid Injections
    Medical condition: Capsulitis of the Shoulder
    Disease: Version SOC Term Classification Code Term Level
    9.1 10001286 Adhesive capsulitis of shoulder LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: GB (Completed)
    Trial results: View results
    EudraCT Number: 2012-005030-11 Sponsor Protocol Number: 12I-BMT08 Start Date*: 2013-02-11
    Sponsor Name:IBSA INSTITUT BIOCHIMIQUE SA
    Full Title: Multicentre, randomized, double-blind, placebo-controlled clinical trial to evaluate the short-term efficacy and safety of two different treatment regimens of Betamethasone valerate 2.25 mg medicat...
    Medical condition: Chronic Lateral Elbow Tendinopathy and Chronic Midportion (or non-insertional) Achilles Tendinopathy
    Disease: Version SOC Term Classification Code Term Level
    14.1 100000004859 10050471 Achilles tendon pain LLT
    14.1 100000004863 10043258 Tennis elbow LLT
    14.1 100000004859 10000441 Achilles tendonitis LLT
    14.1 100000004863 10024032 Lateral epicondylitis LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: View results
    EudraCT Number: 2015-002343-34 Sponsor Protocol Number: KALK1183 Start Date*: 2015-10-15
    Sponsor Name:Martina Hansens Hospital
    Full Title: Treatment of calcific tendinitis of the Rotator Cuff A randomized, double blinded, sham controlled, international, multicenter study
    Medical condition: Calcific tendinitis of the shoulder
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NO (Completed)
    Trial results: (No results available)
    EudraCT Number: 2013-004117-40 Sponsor Protocol Number: Q03.13.01 Start Date*: 2013-12-19
    Sponsor Name:Fidia Farmaceutici SpA
    Full Title: Randomized, controlled, double-blinded clinical trial, with open-label extension on the efficacy of ultrasound guided injection of hyaluronic acid (500-730 KDa) (HYALGAN®) versus saline solution in...
    Medical condition: Achilles tendinopathy
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2010-024641-71 Sponsor Protocol Number: 071(D)SC10102 Start Date*: 2011-05-12
    Sponsor Name:ANGELINI
    Full Title: A randomized, multicenter, double-blind study assessing the efficacy and safety of two topical 10% naproxen gel formulations in the treatment of benign soft-tissue injuries.
    Medical condition: Benign soft-tissue injuries.
    Disease: Version SOC Term Classification Code Term Level
    13.1 10028395 - Musculoskeletal and connective tissue disorders 10028391 Musculoskeletal pain PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: View results
    EudraCT Number: 2012-001056-19 Sponsor Protocol Number: HUPA-EC-02-2012 Start Date*: 2013-12-01
    Sponsor Name:FUNDACIÓN PARA LA INVESTIGACIÓN BIOMÉDICA DEL HOSPITAL UNIVERSITARIO PRÍNCIPE DE ASTURIAS
    Full Title: ROLE OF BIOLOGICAL THERAPY IN ROTATOR CUFF TENDINOPATHY. EFFECTIVENESS OF PLASMA RICH IN GROWTH FACTOR (PRGF-ENDORET)REGARDING TO FUNCTIONAL CAPACITY AND PAIN COMPARED WITH THE CONVENTIONAL TREATME...
    Medical condition: ROTATOR CUFF TENDINOPATHY
    Disease: Version SOC Term Classification Code Term Level
    14.1 100000004859 10039226 Rotator cuff injury LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: ES (Completed)
    Trial results: (No results available)
    EudraCT Number: 2018-004734-15 Sponsor Protocol Number: EBio Start Date*: 2019-06-03
    Sponsor Name:Universitätsklinikum Erlangen
    Full Title: EBIO – Enthesitis biopsy study
    Medical condition: Psoriatic arthritis
    Disease: Version SOC Term Classification Code Term Level
    21.0 100000004859 10037160 Psoriatic arthritis LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2007-001863-31 Sponsor Protocol Number: LR-07 Start Date*: 2009-03-12
    Sponsor Name:Hospital Universitario de Bellvitge
    Full Title: Estudio Comparativo de la Eficacia de Pautas “Cortas” y “Largas” de la Combinación Rifampicina-Levofloxacino en la Infección Estafilocócica Postquirúrgica Precoz y Hematógena de Prótesis Articular ...
    Medical condition: El tratamiento de elección de la infección precoz postquirúrgica y hematógena de prótesis articular con implante estable es el desbridamiento precoz con retención del material y un tratamiento anti...
    Disease: Version SOC Term Classification Code Term Level
    9.1 10021795 Infection and inflammatory reaction due to internal joint prosthesis LLT
    9.1 10065011 Prosthesis related infection LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: ES (Prematurely Ended)
    Trial results: (No results available)
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    The status and protocol content of GB trials is no longer updated since 1 January 2021. For the UK, as of 31 January 2021, EU Law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland/NI. Legal notice
    As of 31 January 2023, all EU/EEA initial clinical trial applications must be submitted through CTIS . Updated EudraCT trials information and information on PIP/Art 46 trials conducted exclusively in third countries continues to be submitted through EudraCT and published on this website.

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